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Clinical Study Manager Jobs in Missouri (NOW HIRING)

Washington University of St. Louis

  • Medical

  • Retirement

  • PTO

Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines ... Evaluates and interprets collected clinical data as appropriate; prepares oral or written ...

University of Rochester

$64K - $96K/yr

The Clinical Trials Project Manager II for NCORP is responsible for leading the planning ... Track study-specific metrics (i.e., overdue data, open queries, etc.) and ensures issues are ...

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$27

$58

$90

How much do clinical study manager jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for clinical study manager in Missouri is $58.64, according to ZipRecruiter salary data. Most workers in this role earn between $47.60 and $66.06 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical study manager?

To thrive as a Clinical Study Manager, you need a strong background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications like GCP (Good Clinical Practice) are highly valued. Strong organizational, leadership, and communication skills help manage cross-functional teams and ensure study timelines are met. These skills are crucial for maintaining study quality, ensuring regulatory adherence, and delivering successful trial outcomes.

What are some common challenges faced by clinical study managers, and how can they be addressed?

Clinical Study Managers often encounter challenges such as coordinating multiple stakeholders, ensuring regulatory compliance, and managing tight timelines across study sites. Effective communication and proactive planning are essential to address these issues, as well as staying up to date with changing industry regulations. Building strong relationships with site staff and fostering a collaborative team environment can also help mitigate delays and ensure study milestones are met successfully.

What are popular job titles related to Clinical Study Manager jobs in Missouri?

For Clinical Study Manager jobs in Missouri, the most frequently searched job titles are:

What job categories do people searching Clinical Study Manager jobs in Missouri look for?

The top searched job categories for Clinical Study Manager jobs in Missouri are:

What cities in Missouri are hiring for Clinical Study Manager jobs?

Cities in Missouri with the most Clinical Study Manager job openings:

Clinical Study Manager jobs near you
Infographic showing various Clinical Study Manager job openings in Missouri as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 10% Part Time, and 1% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $121,973 per year, or $58.6 per hour.

Senior Scientist, Clinical Research

Jobtailor

California, MO • On-site

$120 - $180/hr

Other

Posted yesterday

New

Job description

  • The Early Clinical Scientist (ECS) coordinates the design, planning and execution of early phase clinical trials with the Clinical Director, and internal/external team members.
  • Oversees trials within and/or across program(s)/therapeutic areas and ensures excellence in execution/compliance to support study objectives and data validity.
  • Manages internal/external team performance to achieve project objectives and resolves project performance issues if they arise.
  • Ensures appropriate clinical safety assessment and risk management of compounds.
  • Conducts real-time oversight of ongoing trials to identify and mitigate patient, study design, data or study conduct issues.
  • Reviews and interprets clinical trial data.
  • May conduct on-site study monitoring, including site training & supervision of complex, novel endpoint/biomarker collection processes.
  • Applies thorough knowledge of GCP, ICH guidelines and regulatory requirements for clinical development.
  • Represents Early Stage Development on cross-functional teams to develop and/or improve internal job aids/SOP/clinical development procedures.
  • Identifies and communicates best practices within the organization.
  • Promotes departmental adaptation of new procedures.
  • Co-authors clinical sections of protocols, clinical investigator brochures, clinical study reports, Worldwide Marketing Application/Common Technical Document (WMA/CTD) subsections, and regulatory agency update and safety reports, as well as clinical development plans, publications, and abstracts.
  • Ensures documents are completed in accordance with applicable standards.
  • Develops study operational documents with input from team members (e.g. site monitoring plan, study operations manual, informed consent, etc.).
  • Manages trial and program projects including team activities (i.e. meetings, document/collaborative workspace management, etc.), provides risk assessment and contingency planning, under accelerated timelines.
Requirements
  • At least 3 years experience in an operational clinical scientist or study manager role in clinical research at a pharmaceutical or biotech company.
  • Understanding of clinical research development process from program planning to regulatory submission
  • Able to quickly develop a working scientific knowledge of different therapeutic areas
  • Ability to manage complex operations and projects under accelerated timelines
  • Scientific, medical and/or safety writing and reporting (at least one is required)
  • Ability to partner effectively with internal and external teams to achieve results
  • Knowledge of GCP, ICH guidelines and regulatory requirements
Core Competencies

Demonstrates expertise in managing early phase clinical trials, ensuring compliance with GCP and ICH guidelines, and effectively collaborating with cross-functional teams to achieve project objectives. Proficient in scientific writing and regulatory submissions, with a strong ability to assess clinical safety and manage complex operations under tight timelines.

Highest-signal resume keywords
  • Clinical Trial Management
  • GCP Compliance
  • ICH Guidelines Knowledge
  • Scientific Writing
  • Cross-Functional Collaboration
ATS Optimization Keywords Hard Skills
  • Clinical Trial Design
  • Data Interpretation
  • Risk Management
  • Study Monitoring
  • Operational Document Development
Soft Skills
  • Team Management
  • Problem Solving
  • Effective Communication
Industry Keywords
  • Clinical Research
  • Pharmaceutical
  • Biotech
  • Regulatory Submission
  • Therapeutic Areas
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